TERMIUM Plus®

The Government of Canada’s terminology and linguistic data bank.

PKU [5 records]

Record 1 2017-08-23

English

Subject field(s)
  • Organizations, Administrative Units and Committees
  • General Medicine, Hygiene and Health
OBS

Mission: To improve the lives of people with phenylketonuria (PKU) and allied disorders and the lives of their families. Allied disorders refers to other rare, inherited metabolic disorders also detected by newborn screening.

Key term(s)
  • Canadian PKU and Allied Disorders

French

Domaine(s)
  • Organismes, unités administratives et comités
  • Médecine générale, hygiène et santé

Spanish

Save record 1

Record 2 2011-09-13

English

Subject field(s)
  • Biochemistry
OBS

Term(s) taken from a Canadian laboratory-equipment company's catalogue.

French

Domaine(s)
  • Biochimie
OBS

Terme(s) tiré(s) du catalogue d'une compagnie canadienne d'équipement de laboratoire.

Spanish

Save record 2

Record 3 2011-09-13

English

Subject field(s)
  • Medical and Surgical Equipment
  • Bioengineering
  • Blood
OBS

Term(s) taken from a Canadian laboratory-equipment company's catalogue.

French

Domaine(s)
  • Équipement médico-chirurgical
  • Technique biologique
  • Sang
OBS

Terme(s) tiré(s) du catalogue d'une compagnie canadienne d'équipement de laboratoire.

Spanish

Save record 3

Record 4 2011-09-13

English

Subject field(s)
  • Biochemistry
OBS

Term(s) taken from a Canadian laboratory-equipment company's catalogue.

French

Domaine(s)
  • Biochimie
OBS

Terme(s) tiré(s) du catalogue d'une compagnie canadienne d'équipement de laboratoire.

Spanish

Save record 4

Record 5 2002-03-21

English

Subject field(s)
  • Endocrine System and Metabolism
CONT

Phenylketonuria was first described as a clinical entity in 1934 by Asjborn Fölling, who surmised that the disorder was autosomal recessive and an inborn error of metabolism. ... Phenylketonuria [is] a generic term for severe hyperphenylalaninemia (>1 mM), low phenylalanine tolerance (<500 mg per day), and high risk of mental retardation in the absence of treatment

French

Domaine(s)
  • Systèmes endocrinien et métabolique
CONT

La phénylcétonurie est une maladie génétique héréditaire transmise par les deux parents (porteurs sains) à leur enfant. Elle provient d'un trouble de la transformation de la phénylalanine en tyrosine.

Spanish

Campo(s) temático(s)
  • Sistemas endocrino y metabólico
Save record 5

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